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Head of Regulatory Affairs, FDA Submissions

Employer
NonStop Consulting
Location
Zug
Salary
£141354 - £180619 per annum + Bonus, Share options
Closing date
Jun 23, 2017

View more

Sector
Pharmaceutical, Regulatory Affairs
Contract Type
Employee
Hours
Full Time
Organization Type
Clinical Practice
Jobseeker Type
Professional

Job Details

Regulatory Affairs Director, NDA Submission, Zurich/Zug, Highly Successful Pharmaceutical Company, Switzerland

Interested in taking the lead on a new NDA submission? I am working with a fast growing pharma company who are looking to expand their regulatory team due to an internal promotion. As well as having a product in late stages, the company also have a solid product line that is already on the market. What we are looking for is someone looking for a new challenge, with experience of the FDA, who can manage both pre and post approvals. The company are very commercial; fast paced and are looking to build on their considerable success to date. Please contact me for further information.

Key Responsibilities:

  • LCM for pharma Rx products currently on the market
  • Play a leading role for an NDA
  • Management of a small team
  • Hands on input for submissions of critical regulatory documents
  • Overall a part of the business due diligence team

Key Requirements:

  • Over 8 years experience in pharmaceutical regulatory affairs
  • Fluency in English
  • Life science degree
  • Experience working on Pharmaceutical submissions to the US

For a confidential discussion about regulatory affairs, or to apply, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41435 080817. For regular job updates and market information please join the Switzerland regulatory affairs linked-in group. https://www.linkedin.com/groups/4550988

I am a specialist head hunter(recruiter) for regulatory affairs in the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on the Swiss regulatory affairs market as well as ATMP(Advanced Therapeutics) and biological regulatory professionals world wide. Please refer to ch.linkedin.com/in/regulatoryaffairsswitzerland for references.

Specialties: *Switzerland Regulatory Affairs Market with a focus on German speakers *Biologics EU wide *Module 3, e-CTD, Chemistry Manufacturing and Controls(CMC) *ATMP, ATP, AT, Advanced Therapeutics, World Wide *Recruitment at all levels including associate, manager, senior manager, associate director, director, global director, senior director and vice president. *SwissMedic candidates

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
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